Downloaded from bmj.com on 12 June 2006 Clinical experience, performance in final examinations, and learning style in medical students: prospective study I C McManus, P Richards, B C Winder and K A Sproston BMJ 1998;316;345-350 Updated information and services can be found at: http://bmj.com/cgi/content/full/316/7128/345 These include: References This article cites 26 articles, 4 of which can be accessed free at: http://bmj.com/cgi/content/full/316/7128/345#BIBL 10 online articles that cite this article can be accessed at: http://bmj.com/cgi/content/full/316/7128/345#otherarticles Rapid responses Email alerting service Topic collections You can respond to this article at: http://bmj.com/cgi/eletter-submit/316/7128/345 Receive free email alerts when new articles cite this article - sign up in the box at the top right corner of the article Articles on similar topics can be found in the following collections Undergraduate (226 articles) Notes To order reprints of this article go to: http://www.bmjjournals.com/cgi/reprintform To subscribe to BMJ go to: http://bmj.bmjjournals.com/subscriptions/subscribe.shtml Papers Downloaded from bmj.com on 12 June 2006 Key messages + Children in hospital are often treated with drugs not specifically licensed for use in children (unlicensed), and drugs are also used outside the terms of the product licence that apply to indication, age, dose, or route of administration (off label prescribing) + In this study 36% of children in 707 admissions received drugs prescribed in either an unlicensed or off label manner + Off label drug prescribing was more common than unlicensed drug prescribing + All drugs used to treat children should be subjected to the licensing process to ensure their quality, safety, and efficacy + The Medicines Control Agency, the pharmaceutical industry, and the NHS need to address the issue of drugs being used in these ways Contributors: IC initiated and designed the study, supervised the collection of data, analysed the data, and was involved in writing the paper. ST designed the data collection forms, coordinated and was involved in collecting and analysing the data, and was involved in writing the paper. AJN initiated and was involved in the design of the study, analysed the data, and was involved in writing the paper. AL helped design the data collection form, helped collect the data, and entered the data on to the computer. Funding: North West Regional Health Authority. Conflict of interest: None. 1 2 3 4 5 6 7 8 has established paediatric pharmacology research units, which has resulted in an increase in the number of clinical trials in children (S Yaffe, personal communication, 1997). Each unit is led by an experienced paediatric clinical pharmacologist. The development of a similar approach in the United Kingdom should be encouraged. The establishment of a national centre to study drug treatment in children would increase the number of clinical trials in which children participate. Funding for such a centre should be a priority for the British pharmaceutical industry, the Medicines Control Agency, the NHS, and research charities. 9 10 11 12 13 14 Choonara I, Nunn T, Hull D. Medicines for children. J Pharm Med 1995;5:96. British Paediatric Association and the Association of the British Pharmaceutical Industry. Licensing medicines for children. Joint report of the British Paediatric Association and the Association of the British Pharmaceutical Industry, 1996. London: BPA, 1996. Turner S, Nunn AJ, Choonara I. Unlicensed drug use in children in the UK. Paediatr Perinat Drug Ther 1997;1:52-5. Nahata MC. Licensing of medicines for children in the USA. Paediatr Perinat Drug Ther 1997;1:50-1. Cotè CJ, Kauffman RE, Troendle GJ, Lambert GH. Is the “therapeutic orphan” about to be adopted? Pediatrics 1996;98:118-23. Turner S, Gill A, Nunn T, Hewitt B, Choonara I. Use of “off-label” and unlicensed drugs in paediatric intensive care unit. Lancet 1996;347: 549-50. Association of the British Pharmaceutical Industry. ABPI data sheet compendium 1995-96. London: Datapharm Publications, 1995. British Medical Association and the Royal Pharmaceutical Society of Great Britain. British national formulary. No 31. London: BMA, RPSGB, 1996. Kauffman RE. Status of drug approval processes and regulation of medications for children. Curr Opinion Pediatr 1995;7:195-8. Cotè CJ. Sedation for procedures in children. Paediatr Perinat Drug Ther 1997;1:3-8. European Agency for the Evaluation of Medicinal Products. Note for guidance on clinical investigation of medicinal products in children. London: EAEMP, 1997. Cornelissen EAM, Kollee LAA, De Abreu RA, Motohara K, Monnens LAH. Effects of oral and intramuscular vitamin K prophylaxis on vitamin K1, PIVKA-II and clotting factors in breast fed infants. Arch Dis Child 1992;67:1250-4. Benini F, Johnston C, Faucher D, Aranda JV. Topical anesthesia during circumcision in newborn infants. JAMA 1993;270:850-3. Parkinson L, Hughes J, Gill A, Billingham I, Ratcliffe J, Choonara I. A randomised controlled trial of sedation in the critically ill. Pediatr Anesth 1997;7:405-10. (Accepted 23 September 1997) Clinical experience, performance in final examinations, and learning style in medical students: prospective study I C McManus, P Richards, B C Winder, K A Sproston Abstract Objective: To assess whether the clinical experience of undergraduate medical students relates to their performance in final examinations and whether learning styles relate either to final examination performance or to the extent of clinical experience. Design: Prospective, longitudinal study of two cohorts of medical students assessed by questionnaire at time of application to medical school and by questionnaire and university examination at the end of their final clinical year. Subjects: Two cohorts of students who had applied to St Mary’s Hospital Medical School during 1980 (n = 1478) and 1985 (n = 2399) for admission in 1981 and 1986 respectively. Students in these cohorts who entered any medical school in the United Kingdom were followed up in their final clinical year in 1986-7 and 1991-2. BMJ VOLUME 316 31 JANUARY 1998 Main outcome measures: Students’ clinical experience of a range of acute medical conditions, surgical operations, and practical procedures as assessed by questionnaire in the final year, and final examination results for the students taking their examinations at the University of London. Results: Success in the final examination was not related to a student’s clinical experiences. The amount of knowledge gained from clinical experience was, however, related to strategic and deep learning styles both in the final year and also at the time of application, five or six years earlier. Grades in A level examinations did not relate either to study habits or to clinical experience. Success in the final examination was also related to a strategic or deep learning style in the final year (although not at time of entry to medical school). Conclusions: The lack of correlation between examination performance and clinical experience Academic Department of Psychiatry, Imperial College School of Medicine at St Mary’s, London W2 1PG I C McManus, professor of psychology and medical education B C Winder, research coordinator K A Sproston, research assistant continued over BMJ 1998;316:345–50 345 Papers Northwick Park and St Mark’s Trust, Northwick Park Hospital, Harrow HA1 3UJ P Richards, medical director Correspondence to: Professor I C McManus, Centre for Health Informatics and Multiprofessional Education, University College London Medical School, London N19 5NF i.mcmanus@ ucl.ac.uk Downloaded from bmj.com on 12 June 2006 final year of undergraduate training in the United calls into question the validity of final examinations. Kingdom confirmed that there were large individual How much knowledge is gained from clinical differences in clinical experience as well as secular experience as a student is able to be predicted from trends and regional differences.12 measures of study habits made at the time of application to medical school, some six years earlier, A levels and other secondary school examinations although not from results of A level examinations. are comparatively poor predictors of students’ success Medical schools wishing to select students who will at university.13 Better predictors are students’ gain the most knowledge from clinical experience approaches to their work, or their study habits and cannot use the results of A level examinations alone learning styles.14 15 The skills needed to do well at A but could assess a student’s learning style. level are less sophisticated than the critical analytical skills that universities instil, and the higher correlation between entry qualifications and final grades in science Introduction and medicine than in other university subjects13 “To study the phenomena of disease without books suggests an undue emphasis on factual recall rather is to sail an uncharted sea, while to study books than deeper cognitive analysis. Universities generally without patients is not to go to sea at all.” value deep learning (table 1) that is motivated by a 1 Sir William Osler desire for personal understanding and vocational relevance and demonstrated by the student’s searching Medical training—and particularly British medical for principles and the integration of knowledge across 2–5 training —has always emphasised not merely learning different domains. In contrast, surface learning is motifrom textbooks but also gaining experience directly vated principally by fear of failure and is dominated by from patients themselves. Although clinical experience rote learning for regurgitation in examinations and is is perceived as central to medical education, there has followed by forgetting. Strategic learning is motivated been little assessment of how and why medical students by a desire for success and by competition with other differ in the knowledge they gain from clinical students. In strategic learning students use whichever experience and how clinical experience relates to sucmethod—deep or surface learning—is more appropri6 cess in clinical examinations. Educational theory ate for a particular topic; the result is patchy predicts that clinical experience and examination sucunderstanding and a lack of integration across topics. 7 cess should both relate to study habits. There are large Empirically, deep and strategic learning styles predict variations between students in the amount and range success in final examinations at university, whereas surof their experience,8 9 and differences also occur in face learning predicts failure.15 16 10 11 postgraduate training. Comparison of entry This paper assesses the relation between clinical cohorts of medical students in 1981 and 1986 in their experience, examination success, and study habits in two cohorts of medical students. Table 1 Summary of the differences in motivation and study process in surface, deep, and strategic learning Learning style Motivation Process Surface Completion of course Fear of failure Rote learning of facts and ideas Focus on discrete task components Little real interest in content Deep Interest in subject Vocational relevance Personal understanding Relate ideas to evidence Integrate material across courses Identify general principles Strategic To achieve high grades To compete with others To be successful Use techniques that achieve highest grades Patchy and variable understanding 1980 (1985) Survey of all applicants to St Mary's Hospital Medical School Applicants' questionnaire, which included measures of study habits, sent to all applicants with postal addresses in the United Kingdom (European Community) 85% (93%) response rate 1981 (1986): 517 (871) students admitted to medical schools in the United Kingdom 1986-7 (1991-2): 463 (761) students in their final year at medical schools in the United Kingdom Final year questionnaire, which included questions on clinical experience and study habits, sent to all final year students; 65% (51%) response rate Detailed final examination results collected for all 330 (361) students taking final examination of the University of London Fig 1 Study design for survey of learning styles and clinical experience in two cohorts of medical students in 1981 (1986) 346 Subjects and methods Study design—This study began as two surveys of medical student selection and assessed applicants who had applied for admission to St Mary’s Hospital Medical School in 198117 and 1986 (fig 1).18 All applicants with addresses in the United Kingdom in the first study and addresses in the European Community in the second study were sent a questionnaire which included measures of study habits; there was a response rate of 85% (1151/1362) in the first study and 92% (2043/2209) in the second. Of the 1478 applicants in the first study, 517 were admitted to medical schools in the United Kingdom. Of the 2399 applicants in the second study, 871 were admitted to medical schools in the United Kingdom. In 1986-7, 463 final year students from the first cohort were sent a second questionnaire, as were 761 from the second in 1991-2; the questionnaire measured study habits and clinical experience, and the response rate was 65% (301/461) for the first study and 50% (383/766) for the second. Study habits and learning styles—Members of the two cohorts received an abbreviated 18 item study process questionnaire developed by Biggs19–22 which assesses learning styles on surface, deep, and strategic scales.7 Reliability coefficients (á) were 0.535, 0.737, and 0.703 in final year students in the first study and 0.567, 0.715, and 0.701 for final year students in the second study. For applicants in 1986 the reliability coefficients were 0.556, 0.713, and 0.647. Applicants in 1981 were BMJ VOLUME 316 31 JANUARY 1998 Papers Clinical experience Downloaded from bmj.com on 12 June 2006 assessed on the less reliable measure of syllabus220 boundness23 (á = 0.497). Performance in final examinations—Altogether, 330 of 210 the students in the first cohort and 361 of those in the second took final examinations at the University of 200 London. Detailed information was obtained from 190 records in the faculty of medicine. The examination had five separate sections (medicine, which included 180 psychiatry, paediatrics, and public health; surgery; pathology; clinical pharmacology; and obstetrics and 170 gynaecology), all of which had multiple choice and 160 essay questions. All subjects except pathology had an oral examination (viva voce), and all except clinical 150 pharmacology had a practical or clinical examination or both. Principal component analysis, based on a can140 didate’s individual scores, was used to calculate a single 130 measure of performance, the overall finals score (first cohort: á = 0.879; second cohort: á = 0.868).24 Addi120 tionally, scores were calculated for the five separate subjects and the four modes of assessment (multiple 110 50 60 70 80 90 100 110 120 130 140 150 choice question, essay, oral, and clinical and practical Performance in final examination examinations).24 Clinical experience—Students in the first cohort Fig 2 Association between performance in final examination and total amount of clinical experience in 1986 cohort (r=−0.024, reported their experience of 15 acute medical P=0.75). The measure of clinical experience12 comprised 20 items conditions and those in the second cohort of 20 condiscored 1 to 3 and 47 items scored 1 to 4 (total possible range 67 to tions. Students in each cohort reported their 230). Performance in the final examination was the principal experience of 18 surgical operations. Students in the component of the examinations, scaled to have a mean of 100 and a standard deviation of 15 first cohort reported their experience of 17 practical procedures, and those in the second cohort reported their experience of 29 practical procedures. Scores on the 50 items in the first cohort and 67 in the second expected directions. The pattern was similar for differwere combined into a single total experience score ent subjects and examination methods. Although study 12 (first cohort: á = 0.861; second cohort: á = 0.907). habits in the final year predicted performance in the final examination in the 1986 cohort (n = 344) there Results were non-significant correlations between examination performance and surface, deep, and strategic processClinical experience and final examination ing as assessed at the time of application (r = − 0.068, performance P = 0.21; r = 0.031, P = 0.57; r = − 0.004, P = 0.94). The correlation between overall performance in final Similarly, syllabus-boundness at time of application in examinations and total clinical experience was not sigthe 1981 cohort (n = 285) showed a non-significant nificant (first cohort: r = 0.048, P = 0.48, n = 215; correlation with examination performance second cohort: r = − 0.024, P = 0.75, n = 176) (fig 2). (r = − 0.007, P = 0.90). There was no evidence of specific associations. There Measures of surface, deep, and strategic learning at were non-significant correlations between experience application and in the final year were correlated in the of treating medical conditions and performance on the 1986 cohort (n = 361) (r = 0.420, r = 0.370, r = 0.336 medicine section of the final examination (first cohort: (all P < .001)), confirming moderate long term trait star = − 0.041, P = 0.55; second cohort: r = − 0.059, bility. Syllabus-boundness at time of application in the P = 0.44); between surgical operations seen and 1981 cohort (n = 307) correlated with final year performance in the surgery examination (first cohort: r = 0.088, P = 0.20; second cohort: r = − 0.118, surface, deep, and strategic learning (r = 0.205, P = 0.12); and between overall experience and perP < 0.001; r = − 0.175, P = 0.002 ; r = − 0.039, P = 0.49), formance in clinical examinations (first cohort: confirming construct overlap of syllabus-boundness r = 0.026, P = 0.70; second cohort: r = − 0.042, and learning style. P = 0.58). These results suggest that clinical experience does not influence performance in final examinations. Study habits and clinical experience Table 2 shows the correlation of clinical experience Study habits and performance in final examination and study habits assessed both in the final year and at Study habits in the final year predicted overall examinthe time of application. Students with higher scores on ation performance; the correlations with surface, deep, deep and strategic learning show significantly higher and strategic learning in the first cohort (n = 213) were levels of overall experience (fig 3) whether study habits r = − 0.204 (P = 0.003), r = 0.157 (P = 0.022), and are measured in the final year or at the time of r = 0.178 (P = 0.009) respectively and in the second selection—five or six years earlier. Surface learning cohort (n = 171) r = − 0.081 (P = 0.28), r = 0.235 (and syllabus-boundness) scores at application showed (P = 0.002), and r = 0.266 (P < 0.001). The negative significant negative correlations with clinical associations with surface learning and positive associations with deep and strategic learning were in the experience. BMJ VOLUME 316 31 JANUARY 1998 347 Papers Clinical experience Downloaded from bmj.com on 12 June 2006 Non-respondents Table 2 Correlation (r) between amount of clinical experience A potential risk in a study in which only 51% of and measures of study habits assessed at time of application students in the first cohort and 65% in the second and in final year in 1981 and 1986 cohorts replied to the questionnaire during their final year is At application In final year that respondents may represent a biased subset of 1981 cohort those in the initial study. In the initial study, however, No of respondents 311 333 this bias is unlikely to be a serious problem since Syllabus-boundness −0.134* NE response rates were satisfactory at 85% and 93% Surface learning NE −0.073 respectively. We assessed possible bias by comparing Deep learning NE 0.212*** baseline measures and the final examination performStrategic learning NE 0.206*** ance of those who did and those who did not return 1986 cohort our questionnaire during their final year. In neither No of respondents 363 375 cohort were there significant differences between Surface learning −0.140** −0.054 Deep learning 0.262*** 0.136** respondents and non-respondents in the final year in Strategic learning 0.220*** 0.213*** terms of study habits at the time of selection, final year *P<0.05; **P<0.01; ***P<0.001. examination performance, or in mean grade at O level, NE=Not evaluated. and number of O and A levels taken. In the 1981 cohort the non-respondents had slightly lower mean grades at A level (3.81 (SD 0.77), n = 177 v 3.98 (0.78), 220 t = 2.44, df = 513, P = 0.015); the effect was not 210 significant in the 1986 cohort (4.16 (0.741), n = 377 v 4.19 (0.64), t = 0.67, df = 513, P = 0.051). Our respond200 ents were probably a representative sample of the stu190 dents as a whole. 180 170 Discussion 160 150 140 130 120 110 100 90 80 5 10 15 20 25 30 35 Deep learning score on application Fig 3 Association between total amount of clinical experience and score on Biggs’s measure of deep learning in applicants in the 1986 cohort (r=0.262, P<0.001). Clinical experience measured as in fig 2 A level examinations Grades at A level are a potential confounder of the associations reported here. Mean A level grade17 18 showed a significant correlation with performance in final examinations (first cohort: r = 0.336, P < 0.001, n = 329; second cohort: r = 0.281, P < 0.001, n = 359); these values are compatible with those reported elsewhere.25 26 However, grades at A level showed almost no association with syllabus-boundness in the 1981 cohort (r = 0.047, P = 0.12, n = 1104) and with surface, deep, and strategic learning at the time of selection in the second cohort (r = − 0.021, P = 0.34; r = − 0.051, P = 0.024; r = 0.024, P = 0.29; n = 1932, NS). There was no correlation with learning styles in the final year (first cohort (n = 333): r = − 0.076, P = 0.26 for surface learning; r = 0.080, P = 0.15 for deep learning; r = 0.099, P = 0.07 for strategic learning; second cohort (n = 371): r = 0.091, P = 0.080; r = -0.005, P = 0.93; r = 0.003, P = 0.96); grades at A level did not correlate with clinical experience (first cohort: r = 0.023, P = 0.68, n = 335; second cohort: r = − 0.034, P = 0.51, n = 370). 348 Medical students work hard to acquire clinical experience.27 If clinical problem solving is the key to learning for medical students and doctors,28 potential doctors should see many patients and medical students with clinical experience should be seen to benefit from it, not least by performing better in clinical examinations. If clinical experience is educationally desirable then students who are likely to learn most from their contact with patients should be selected to study medicine. Validity of final examinations Our study shows that students with more clinical experience do not do better in final examinations either generally or specifically in the clinical sections of examinations. This conclusion is robust, being found in two cohorts of reasonable size studied five years apart. We do not believe our results reflect any specific failing of the University of London’s examinations, which are typical of those in most medical schools in the United Kingdom and have external examiners at all levels. We also recognise that the radical educational and curricular changes being introduced into medical schools since the publication of Tomorrow’s Doctors by the General Medical Council29 may invalidate our findings for future generations of medical students. That, however, is an empirically testable hypothesis, and our current study provides the baseline data needed for assessing the reforms. The lack of correlation between the amount of clinical experience and performance in final examinations calls into question the clinical validity of the examinations; our conclusions may also apply to similarly structured postgraduate examinations. Examinations may be failing to assess the skills and knowledge acquired directly from clinical experience, such as carrying out practical procedures, communicating with patients, formulating differential diagnoses, ordering tests, evaluating their results, and deciding on manageBMJ VOLUME 316 31 JANUARY 1998 Papers Downloaded from bmj.com on 12 June 2006 throughout a professional career—is a characteristic that Key messages can be identified at the time of selection. However, selection of medical students is based primarily on the results + Medical students with the most clinical of examinations that do not correlate with the learning experience do not perform best in final styles that are desirable in medical students, and these undergraduate examinations, throwing some examinations do not predict the successful acquisition of doubt on the validity of the examinations clinical experience. The implication is that the greater + The amount of knowledge a student gains from the dependence of a selection system on grades at A clinical experience correlates positively with level the more limited is its capacity for selecting doctors deep and strategic learning styles as measured who will gain the most knowledge from clinical not only in the final year but also at the time of experience and therefore probably continue to benefit selection, five or six years earlier from clinical experience throughout their careers.29 + If it is important for students to obtain as much Evaluation of the effectiveness of medical training clinical experience as possible then final should concentrate on characteristics other than the examinations require restructuring to assess ability to pass examinations, both as an input measure and reward clinical experience, and selection for selection and as an output measure of the quality of should emphasise deep learning which cannot medical education. be assessed from grades at A level + The use of deep and strategic learning styles in the final year of medical school predicts better performance in the final examination, but the same measures at the time of selection for admission to medical school do not predict examination performance ment. An alternative possibility is that students are failing to learn properly from their experience since “[clinical] experience without training increases confidence not competence.”30 31 Whatever the mechanism, it must be a concern that examinations send the wrong messages to undergraduates. Assessments determine what and how students choose to study. If skills and experiences acquired from patients are not seen to be relevant to success in examinations then fear of failure will drive some students to ignore clinical experience and resort instead to what is perceived as the real curriculum—that is, the information contained in textbooks. These attitudes seem unlikely to encourage the lifelong learning necessary for doctors, or to foster the development of “reflective practitioner[s]”32 who can modify their practice in relation to experience. Since strategic and deep learning styles correlate positively with performance in final examinations and surface learning correlates negatively, the present examinations are probably encouraging a deeper understanding of medicine and medical practice. That other studies have failed to find this probably indicates that they had too small a sample size.33 That study habits at the time of selection for admission to medical school did not predict results in final examinations reflects the fact that study habits are states as much as traits. There is a well documented trend towards surface learning in conventional medical education,34 35 a process driven in part by failure in previous examinations.36 Courses structured less conventionally, perhaps using problem based learning,34 35 may find a correlation between study habits at entry and performance in final examinations. Clinical experience and study habits An important finding of this study is that the knowledge acquired by a clinical student can be predicted from the learning style measured at the time of application to medical school—half a decade earlier. This implies that the acquisition of knowledge from clinical experience— and the ability to continue to gain experience BMJ VOLUME 316 31 JANUARY 1998 We thank the Faculty of Medicine of the University of London for permission to analyse the examination results of undergraduates, and we thank our many respondents for completing our questionnaires. Contributors: ICM and PR initiated and designed the cohort studies; ICM was responsible for management of the studies and for statistical analysis; BCW coordinated the acquisition and processing of the data; KAS and BCW collected much of the data; the manuscript was written by ICM and PR with help from BCW and KAS. ICM is guarantor for this paper. Funding: The survey of the 1981 cohort was funded by the Economic and Social Research Council, and the survey of the 1986 cohort by the Economic and Social Research Council and the Leverhulme Trust. Conflict of interest: None. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 Salter RH. Stop denigrating service. BMJ 1995;310:538. Flexner A. Medical education: a comparative study. New York: MacMillan, 1925. Pickering G. Quest for excellence in medical education: a personal survey. Oxford: Oxford University Press, 1978. Sinclair D. Basic medical education. London: Oxford University Press, 1972. Bonner TN. Becoming a physician: medical education in Great Britain, France, Germany, and the United States, 1750-1945. New York: Oxford University Press, 1995. Jolly BC, Jones A, Dacre JE, Elzubeir M, Kopelman P, Hitman G. Relationships between students’ clinical experiences in introductory clinical courses and their performances on an objective structured clinical examination (OSCE). 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(Accepted 5 August 1997) Home sampling versus conventional contact tracing for detecting Chlamydia trachomatis infection in male partners of infected women: randomised study Berit Andersen, Lars Østergaard, Jens K Møller, Frede Olesen See p 351 Research Unit and Department of General Practice, University of Aarhus, DK-8000 Aarhus C, Denmark Berit Andersen, research assistant Frede Olesen, consultant physician Aarhus University Hospital, DK-8000 Aarhus C Lars Østergaard, senior registrar of infectious diseases Jens K Møller, director of clinical microbiology Correspondence to: Dr Andersen ba@alm.aau.dk BMJ 1998;316:350–1 350 Urogenital infections with Chlamydia trachomatis are widespread and usually asymptomatic. Major complications from infection include ectopic pregnancies and female infertility.1 Although contact tracing reduces the prevalence of chlamydia infection,2 the test rate among partners is often low, partly because male contacts have to have a urethral swab taken by a doctor. As the polymerase chain reaction can successfully detect infection in urine samples,3 we investigated whether the test rate could be increased by asking the male contacts of infected women to send a urine sample directly from home to a laboratory instead of having a doctor take a urethral swab. Subjects, methods, and results Ninety six women with C trachomatis infection seen in general practices in Aarhus County, Denmark, were randomly divided according to their date of birth into an intervention group (45 patients) and a control group (51 patients). Women in the intervention group were asked to complete a questionnaire, including the number of male sexual partners over the preceding six months, and to supply their partners with an envelope containing a 10 ml sterile container, information on collecting the first urine sample of the morning, and a prepaid envelope for returning the sample to the laboratory at the Aarhus University Hospital. Envelopes supplied by the control group contained a request for the partner to visit his doctor as well as a contact slip and a prepaid envelope to be given to the doctor for returning a urethral swab sample. Swab samples were examined by enzyme immunoassay (MicroTrak II, Behring, Germany). Specimens with an optical density greater than 30% of the recommended cut off point were confirmed by polymerase chain reaction assay (Amplicor, Roche, Switzerland).4 Urine samples were analysed by the same polymerase chain reaction. A sample was considered positive only if the result was confirmed on retesting. The table shows the results of contact tracing. Forty four out of 65 (68%) partners were examined in the intervention group compared with 19 out of 68 (28%) in the control group (÷2 = 19.50; P < 0.01). The difference in test rate was 0.4 (0.68 minus 0.28) (95% confidence interval 0.24 to 0.56). Although not significant, there were more new cases of C trachomatis per index case in the intervention group (0.27) than in the control group (0.14). The difference between the two groups was 0.13 ( − 0.03 to 0.29). Furthermore, there was a trend for partners of women in the intervention group to be tested earlier than those of women in the control group, with a mean delay time of 12.6 days and 17.7 days respectively. Thus the difference between the two groups was 5.1 days ( − 1.6 to 11.8). The prevalence of C trachomatis in samples from the intervention and control groups was 27% and 39% respectively. Tracing of male contacts of women with Chlamydia trachomatis infection Intervention group (n=45) Control group (n=51) No 65 68 Median No per index case 1 1 Mean No per index case 1.44 1.33 Range 0-4 0-4 Partners contacted Partners tested No (% of those contacted) 44 (68) 19 (28)* Mean No per index case 0.98 0.37 Range 0-3 0-1 No (% of those tested) 12(27) 7(39) Mean No per index case 0.27 0.14 12.6 17.7 Partners infected Time until testing Mean delay (days) *Result unknown for one partner. BMJ VOLUME 316 31 JANUARY 1998